myMedidata

Clinical trials ask a lot of patients. Clinical trial participation shouldn’t make it harder.

myMedidata is a single patient portal built with patients, for patients. It brings all patient trial activities including eCOA, consent, sensors, and payments into one connected experience, so participation stays consistent as trials evolve.

 

One Account, Simplified Participation

myMedidata brings patient participation into a single, consistent experience. One account helps reduce friction for patients, simplify coordination for sites, and support retention across the study.

Patient-centric by Design
Device Agnostic
Trials without Boundaries

Keeping Patients and Sites Aligned

Patients

One Place for All Trial Activities

Eliminate extra apps, logins, and unnecessary steps by giving patients one location for all their clinical trial activities.

myMedidata makes it simple for patients to participate and stay engaged throughout their entire trial journey.

 
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What Comes Together in myMedidata

myMedidata brings together Medidata’s patient-facing solutions in a single experience, so participation, communication, and data collection stay connected throughout the study.
It creates a consistent experience for patients and a unified source of patient data for study teams.

Featured Resource


The Value of Decentralized Clinical Trials

Hear from Medidata’s CEO on how decentralized and hybrid trial models are changing patient participation, site workflows, and study execution, and what that shift means for sponsors planning future studies.

 
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More Resources


Explore deeper guidance and related materials.

View All Resources

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FAQ

Yes. myMedidata is designed as a single-destination patient portal that allows patients to access all clinical trial activities, including learning about trials, consenting, completing questionnaires, and processing payments. This unified approach eliminates the need for multiple logins and applications, streamlining the experience for patients.

Yes. Beyond its accessibility on the web, myMedidata native app is available on both iOS and Android and supports a "Bring Your Own Device" (BYOD) model as well as provisioned devices. 

Yes. myMedidata Registries expands patient participation from a single transaction to a pre-trial and post-trial engagement approach. This allows sponsors to engage and educate patients about their studies, build a pool of pre-qualified prospective participants before their trials start, and follow up post-trial with future trial opportunities.

Through their myMedidata account, patients can access all the tools they need to complete their trial tasks, including consent, eCOA, sensors, payments, and telehealth, on-site or remotely. All data captured through myMedidata flows into Rave EDC, which enables real-time visibility for sites to ensure compliance as well as reduce travel burden for patients. 

Yes. Medidata offers a variety of training options for our clients and partners, including both self-paced and instructor-led courses. To learn more about available courses and to access our resources, please visit the Medidata Global Education and Training section.